Related Experiment Video
Updated: Sep 20, 2025

Acupoint Catgut Embedding Therapy in Traditional Chinese Medicine for Managing Allergic Rhinitis
Published on: December 20, 2024
Advancements in Novel Therapeutics for Chronic Spontaneous Urticaria
Joshua S Bernstein1, Gordon Sussman2, Helena Pite3
1Division of Rheumatology, Allergy, and Immunology, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Abstract:
Chronic urticaria (CU) is defined by pruritic wheals with or without angioedema, associated with severe itch, which persist for greater than 6 weeks. Lesions move from one part of the body to another and generally are evanescent, lasting less than 24 hours. The global prevalence of the disease ranges from 0.5% to 5% and is correlated with an annual economic burden of over $200 million in the United States. Chronic urticaria can be further divided into chronic spontaneous urticaria and chronic inducible urticaria. Whereas chronic spontaneous urticaria has no identifiable trigger, chronic inducible urticaria can be provoked by both physical and nonphysical stimuli. As many as 7% to 30% of patients with CU can have both types. Mast cells are the major effector cells in the pathogenesis of CU. When activated, mast cells characteristically release bioactive mediators including histamine that bind to specific receptors causing vasodilation and extravasation of fluid from the blood vasculature. This causes the characteristic wheals and itch. However, the pathophysiology of CU is much more complex, involving many mast cell surface receptors, cytokines, and cell activation pathways that are targets for many of the currently available and investigational therapies. Studies have demonstrated that CU causes a significant amount of distress and disruption to patients' daily lives that can be evaluated using validated patient-reported outcomes measures. In this review, we review CU epidemiology, pathophysiology, subtypes, and diagnosis and discuss current and novel therapies.
Related Concept Videos
Antiasthma Drugs: Mast Cell Stabilizers and Anti-IgE Drugs
Mast cell stabilizers, such as cromolyn (also known as sodium cromoglycate) and nedocromil (Tilade), are effective drugs in asthma management. These stabilizers hinder histamine release by skillfully obstructing the activation of mast cells and other cellular entities. Notably, they navigate this task without...
Antiasthma Drugs: Leukotriene Modifiers
Leukotriene modifiers work through two distinct mechanisms:
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
Drug Delivery: Miscellaneous Routes
Oral inhalation and nasal sprays swiftly transfer drugs across the respiratory epithelium's mucosal layer. Inhaled glucocorticoids and bronchodilators directly target lung conditions such as asthma, while fluticasone nasal spray mitigates allergic rhinitis.
Transdermal patches transport drugs...
Cholinergic Antagonists: Therapeutic Uses
Respiratory Tract: Ipratropium, aclidinium, and tiotropium treat asthma, chronic bronchitis, and chronic obstructive pulmonary disease (COPD). They protect against bronchoconstriction caused by irritants like cigarette smoke, sulfur dioxide, and ozone. They also help reduce nasopharyngeal...

